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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2298359Generated: October 26, 2026

Thiophenol → Ethyl 2-phenylsulfanyl-thiazole-5-carboxylate

https://huagongshe.com/reaction/2298359

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThiophenolHCID 7969—
ReactantPotassium CarbonateHCID 11430—
ReactantEthyl 2-bromothiazole-5-carboxylateHCID 3614103—
SolventEthanolHCID 702—
ProductEthyl 2-phenylsulfanyl-thiazole-5-carboxylateHCID 1090151948%

Reaction Steps

A suspension of 2-bromo-1,3-thiazole-5-carboxylic acid ethyl ester (1.5 g, 6.15 mmol, 1 eq) and K2CO3 (1.7 g, 12.3 mmol, 2 eq) in EtOH (60 mL) is cooled in an ice bath, and thiophenol (0.631 mL, 6.15 mmol, 1 eq) is added. The reaction is monitored by HPLC until the starting material is consumed. The reaction mixture is filtered (to remove a solid by-product), and the solvent is removed in vacuo. The crude mixture is purified by silica gel chromatography using a Biotage Flash 40S column using 2% EtOAc in hexanes to afford the product as an oil (0.784 g, 46%). MS (ESI) for C12H11NO2S2m/z 266.1 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06492385B2
Source datasetuspto-grants-2002_12
ORD IDord-a30e3ab6e8c841d6ba24668fe2cdf3d3
Source noteuspto-grants-2002_12